Annualized changes in rate of amyloid deposition and neurodegeneration are greater in participants who become amyloid positive than those who remain amyloid negative

This study longitudinally examined participants in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) who underwent a conversion in amyloid-beta (Aβ) status in comparison to a group of ADNI participants who did not show a change in amyloid status over the same follow-up period. Participants incl...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurobiology of aging 2023-07, Vol.127, p.33-42
Hauptverfasser: Groechel, Renée C., Tripodis, Yorghos, Alosco, Michael L., Mez, Jesse, Qiu, Wei Qiao, Mercier, Gustavo, Goldstein, Lee, Budson, Andrew E., Kowall, Neil W., Killiany, Ronald J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 42
container_issue
container_start_page 33
container_title Neurobiology of aging
container_volume 127
creator Groechel, Renée C.
Tripodis, Yorghos
Alosco, Michael L.
Mez, Jesse
Qiu, Wei Qiao
Mercier, Gustavo
Goldstein, Lee
Budson, Andrew E.
Kowall, Neil W.
Killiany, Ronald J.
description This study longitudinally examined participants in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) who underwent a conversion in amyloid-beta (Aβ) status in comparison to a group of ADNI participants who did not show a change in amyloid status over the same follow-up period. Participants included 136 ADNI dementia-free participants with 2 florbetapir positron emission tomography (PET) scans. Of these participants, 68 showed amyloid conversion as measured on florbetapir PET, and the other 68 did not. Amyloid converters and non-converters were chosen to have representative demographic data (age, education, sex, diagnostic status, and race). The amyloid converter group showed increased prevalence of APOE ε4 (p 
doi_str_mv 10.1016/j.neurobiolaging.2023.03.005
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2800627220</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0197458023000519</els_id><sourcerecordid>2800627220</sourcerecordid><originalsourceid>FETCH-LOGICAL-c381t-1d5fcdc8724796d430530d276bf43650e8a9b9ee22b7438a457ddd79e397ac713</originalsourceid><addsrcrecordid>eNqNkcFq3DAQhkVoabbbvkLQoYdevB1JtmVDLyE0bSGQS3sWsjR2tNiSK9kp6fv0PavdTQK9BQYJhu-ff4afkA8MdgxY_Wm_87jG0Lkw6sH5YceBix3kguqMbFhVNQUrW_mKbIC1siirBs7J25T2ACBLWb8h50JCKZqGbcjfS-9XPbo_aKm5037ARJ2nUS9IQ0_19DAGZ6nFOSS3uOCp9pYeN7A4oMdMHrsR6RAxy-JBP-u4OONm7ZdEf98F2qEJEz7PO027R7pkz_yEhEcs4qSz_AnzOOgD9o687vWY8P3jvyU_r7_8uPpW3Nx-_X51eVMY0bClYLbqjTWN5KVsa1sKqARYLuuuL0VdATa67VpEzjuZ79dlJa21skXRSm0kE1vy8TR3juHXimlRk0sGx1F7DGtSvAGoueQcMvr5hJoYUorYqzm6SccHxUAdglJ79X9Q6hCUglx5rS25eHRauwnts_gpmQxcnwDM9947jCoZh96gdRHNomxwL3P6B-FPsdA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2800627220</pqid></control><display><type>article</type><title>Annualized changes in rate of amyloid deposition and neurodegeneration are greater in participants who become amyloid positive than those who remain amyloid negative</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Groechel, Renée C. ; Tripodis, Yorghos ; Alosco, Michael L. ; Mez, Jesse ; Qiu, Wei Qiao ; Mercier, Gustavo ; Goldstein, Lee ; Budson, Andrew E. ; Kowall, Neil W. ; Killiany, Ronald J.</creator><creatorcontrib>Groechel, Renée C. ; Tripodis, Yorghos ; Alosco, Michael L. ; Mez, Jesse ; Qiu, Wei Qiao ; Mercier, Gustavo ; Goldstein, Lee ; Budson, Andrew E. ; Kowall, Neil W. ; Killiany, Ronald J. ; for the Alzheimer’s Disease Neuroimaging Initiative ; Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><description>This study longitudinally examined participants in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) who underwent a conversion in amyloid-beta (Aβ) status in comparison to a group of ADNI participants who did not show a change in amyloid status over the same follow-up period. Participants included 136 ADNI dementia-free participants with 2 florbetapir positron emission tomography (PET) scans. Of these participants, 68 showed amyloid conversion as measured on florbetapir PET, and the other 68 did not. Amyloid converters and non-converters were chosen to have representative demographic data (age, education, sex, diagnostic status, and race). The amyloid converter group showed increased prevalence of APOE ε4 (p &lt; 0.001), greater annualized percent volume loss in selected magnetic resonance imaging (MRI) regions (p &lt; 0.05), lower cerebrospinal fluid Aβ1–42 (p &lt; 0.001), and greater amyloid retention (as measured by standard uptake value ratios) on florbetapir PET scans (p &lt; 0.001) in comparison to the non-converter group. These results provide compelling evidence that important neuropathological changes are occurring alongside amyloid conversion.</description><identifier>ISSN: 0197-4580</identifier><identifier>EISSN: 1558-1497</identifier><identifier>DOI: 10.1016/j.neurobiolaging.2023.03.005</identifier><identifier>PMID: 37043881</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alzheimer Disease - pathology ; Alzheimer’s disease ; Amyloid ; Amyloid beta-Peptides - metabolism ; Aniline Compounds ; Brain - metabolism ; Cognition ; Cognitive Dysfunction - pathology ; Dementia ; Ethylene Glycols ; Humans ; Magnetic resonance imaging ; Positron emission tomography ; Positron-Emission Tomography - methods</subject><ispartof>Neurobiology of aging, 2023-07, Vol.127, p.33-42</ispartof><rights>2023 Elsevier Inc.</rights><rights>Copyright © 2023 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c381t-1d5fcdc8724796d430530d276bf43650e8a9b9ee22b7438a457ddd79e397ac713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neurobiolaging.2023.03.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37043881$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Groechel, Renée C.</creatorcontrib><creatorcontrib>Tripodis, Yorghos</creatorcontrib><creatorcontrib>Alosco, Michael L.</creatorcontrib><creatorcontrib>Mez, Jesse</creatorcontrib><creatorcontrib>Qiu, Wei Qiao</creatorcontrib><creatorcontrib>Mercier, Gustavo</creatorcontrib><creatorcontrib>Goldstein, Lee</creatorcontrib><creatorcontrib>Budson, Andrew E.</creatorcontrib><creatorcontrib>Kowall, Neil W.</creatorcontrib><creatorcontrib>Killiany, Ronald J.</creatorcontrib><creatorcontrib>for the Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><creatorcontrib>Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><title>Annualized changes in rate of amyloid deposition and neurodegeneration are greater in participants who become amyloid positive than those who remain amyloid negative</title><title>Neurobiology of aging</title><addtitle>Neurobiol Aging</addtitle><description>This study longitudinally examined participants in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) who underwent a conversion in amyloid-beta (Aβ) status in comparison to a group of ADNI participants who did not show a change in amyloid status over the same follow-up period. Participants included 136 ADNI dementia-free participants with 2 florbetapir positron emission tomography (PET) scans. Of these participants, 68 showed amyloid conversion as measured on florbetapir PET, and the other 68 did not. Amyloid converters and non-converters were chosen to have representative demographic data (age, education, sex, diagnostic status, and race). The amyloid converter group showed increased prevalence of APOE ε4 (p &lt; 0.001), greater annualized percent volume loss in selected magnetic resonance imaging (MRI) regions (p &lt; 0.05), lower cerebrospinal fluid Aβ1–42 (p &lt; 0.001), and greater amyloid retention (as measured by standard uptake value ratios) on florbetapir PET scans (p &lt; 0.001) in comparison to the non-converter group. These results provide compelling evidence that important neuropathological changes are occurring alongside amyloid conversion.</description><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer’s disease</subject><subject>Amyloid</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Aniline Compounds</subject><subject>Brain - metabolism</subject><subject>Cognition</subject><subject>Cognitive Dysfunction - pathology</subject><subject>Dementia</subject><subject>Ethylene Glycols</subject><subject>Humans</subject><subject>Magnetic resonance imaging</subject><subject>Positron emission tomography</subject><subject>Positron-Emission Tomography - methods</subject><issn>0197-4580</issn><issn>1558-1497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFq3DAQhkVoabbbvkLQoYdevB1JtmVDLyE0bSGQS3sWsjR2tNiSK9kp6fv0PavdTQK9BQYJhu-ff4afkA8MdgxY_Wm_87jG0Lkw6sH5YceBix3kguqMbFhVNQUrW_mKbIC1siirBs7J25T2ACBLWb8h50JCKZqGbcjfS-9XPbo_aKm5037ARJ2nUS9IQ0_19DAGZ6nFOSS3uOCp9pYeN7A4oMdMHrsR6RAxy-JBP-u4OONm7ZdEf98F2qEJEz7PO027R7pkz_yEhEcs4qSz_AnzOOgD9o687vWY8P3jvyU_r7_8uPpW3Nx-_X51eVMY0bClYLbqjTWN5KVsa1sKqARYLuuuL0VdATa67VpEzjuZ79dlJa21skXRSm0kE1vy8TR3juHXimlRk0sGx1F7DGtSvAGoueQcMvr5hJoYUorYqzm6SccHxUAdglJ79X9Q6hCUglx5rS25eHRauwnts_gpmQxcnwDM9947jCoZh96gdRHNomxwL3P6B-FPsdA</recordid><startdate>202307</startdate><enddate>202307</enddate><creator>Groechel, Renée C.</creator><creator>Tripodis, Yorghos</creator><creator>Alosco, Michael L.</creator><creator>Mez, Jesse</creator><creator>Qiu, Wei Qiao</creator><creator>Mercier, Gustavo</creator><creator>Goldstein, Lee</creator><creator>Budson, Andrew E.</creator><creator>Kowall, Neil W.</creator><creator>Killiany, Ronald J.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202307</creationdate><title>Annualized changes in rate of amyloid deposition and neurodegeneration are greater in participants who become amyloid positive than those who remain amyloid negative</title><author>Groechel, Renée C. ; Tripodis, Yorghos ; Alosco, Michael L. ; Mez, Jesse ; Qiu, Wei Qiao ; Mercier, Gustavo ; Goldstein, Lee ; Budson, Andrew E. ; Kowall, Neil W. ; Killiany, Ronald J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-1d5fcdc8724796d430530d276bf43650e8a9b9ee22b7438a457ddd79e397ac713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer’s disease</topic><topic>Amyloid</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Aniline Compounds</topic><topic>Brain - metabolism</topic><topic>Cognition</topic><topic>Cognitive Dysfunction - pathology</topic><topic>Dementia</topic><topic>Ethylene Glycols</topic><topic>Humans</topic><topic>Magnetic resonance imaging</topic><topic>Positron emission tomography</topic><topic>Positron-Emission Tomography - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Groechel, Renée C.</creatorcontrib><creatorcontrib>Tripodis, Yorghos</creatorcontrib><creatorcontrib>Alosco, Michael L.</creatorcontrib><creatorcontrib>Mez, Jesse</creatorcontrib><creatorcontrib>Qiu, Wei Qiao</creatorcontrib><creatorcontrib>Mercier, Gustavo</creatorcontrib><creatorcontrib>Goldstein, Lee</creatorcontrib><creatorcontrib>Budson, Andrew E.</creatorcontrib><creatorcontrib>Kowall, Neil W.</creatorcontrib><creatorcontrib>Killiany, Ronald J.</creatorcontrib><creatorcontrib>for the Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><creatorcontrib>Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Neurobiology of aging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Groechel, Renée C.</au><au>Tripodis, Yorghos</au><au>Alosco, Michael L.</au><au>Mez, Jesse</au><au>Qiu, Wei Qiao</au><au>Mercier, Gustavo</au><au>Goldstein, Lee</au><au>Budson, Andrew E.</au><au>Kowall, Neil W.</au><au>Killiany, Ronald J.</au><aucorp>for the Alzheimer’s Disease Neuroimaging Initiative</aucorp><aucorp>Alzheimer’s Disease Neuroimaging Initiative</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Annualized changes in rate of amyloid deposition and neurodegeneration are greater in participants who become amyloid positive than those who remain amyloid negative</atitle><jtitle>Neurobiology of aging</jtitle><addtitle>Neurobiol Aging</addtitle><date>2023-07</date><risdate>2023</risdate><volume>127</volume><spage>33</spage><epage>42</epage><pages>33-42</pages><issn>0197-4580</issn><eissn>1558-1497</eissn><abstract>This study longitudinally examined participants in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) who underwent a conversion in amyloid-beta (Aβ) status in comparison to a group of ADNI participants who did not show a change in amyloid status over the same follow-up period. Participants included 136 ADNI dementia-free participants with 2 florbetapir positron emission tomography (PET) scans. Of these participants, 68 showed amyloid conversion as measured on florbetapir PET, and the other 68 did not. Amyloid converters and non-converters were chosen to have representative demographic data (age, education, sex, diagnostic status, and race). The amyloid converter group showed increased prevalence of APOE ε4 (p &lt; 0.001), greater annualized percent volume loss in selected magnetic resonance imaging (MRI) regions (p &lt; 0.05), lower cerebrospinal fluid Aβ1–42 (p &lt; 0.001), and greater amyloid retention (as measured by standard uptake value ratios) on florbetapir PET scans (p &lt; 0.001) in comparison to the non-converter group. These results provide compelling evidence that important neuropathological changes are occurring alongside amyloid conversion.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>37043881</pmid><doi>10.1016/j.neurobiolaging.2023.03.005</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0197-4580
ispartof Neurobiology of aging, 2023-07, Vol.127, p.33-42
issn 0197-4580
1558-1497
language eng
recordid cdi_proquest_miscellaneous_2800627220
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Alzheimer Disease - pathology
Alzheimer’s disease
Amyloid
Amyloid beta-Peptides - metabolism
Aniline Compounds
Brain - metabolism
Cognition
Cognitive Dysfunction - pathology
Dementia
Ethylene Glycols
Humans
Magnetic resonance imaging
Positron emission tomography
Positron-Emission Tomography - methods
title Annualized changes in rate of amyloid deposition and neurodegeneration are greater in participants who become amyloid positive than those who remain amyloid negative
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T04%3A54%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Annualized%20changes%20in%20rate%20of%20amyloid%20deposition%20and%20neurodegeneration%20are%20greater%20in%20participants%20who%20become%20amyloid%20positive%20than%20those%20who%20remain%20amyloid%20negative&rft.jtitle=Neurobiology%20of%20aging&rft.au=Groechel,%20Ren%C3%A9e%20C.&rft.aucorp=for%20the%20Alzheimer%E2%80%99s%20Disease%20Neuroimaging%20Initiative&rft.date=2023-07&rft.volume=127&rft.spage=33&rft.epage=42&rft.pages=33-42&rft.issn=0197-4580&rft.eissn=1558-1497&rft_id=info:doi/10.1016/j.neurobiolaging.2023.03.005&rft_dat=%3Cproquest_cross%3E2800627220%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2800627220&rft_id=info:pmid/37043881&rft_els_id=S0197458023000519&rfr_iscdi=true